C2751088[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 426980	NM_001040151.2(SCN3B):c.614A>G (p.Asn205Ser)	SCN3B (N205S)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 642346	NM_001040151.2(SCN3B):c.583G>A (p.Ala195Thr)	SCN3B (A195T)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +3 more	GConflicting classifications of pathogenicity
Select item 190883	NM_001040151.2(SCN3B):c.582C>T (p.Asn194=)	SCN3B	Single nucleotide variant (synonymous variant)	Brugada syndrome 7 +2 more	GBenign/Likely benign
Select item 190888	NM_001040151.2(SCN3B):c.416G>A (p.Arg139Gln)	SCN3B (R139Q)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 644208	NM_001040151.2(SCN3B):c.395G>A (p.Arg132Gln)	SCN3B (R132Q)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +1 more	GUncertain significance
Select item 139033	NM_001040151.2(SCN3B):c.390G>A (p.Ala130=)	SCN3B	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 1444334	NM_001040151.2(SCN3B):c.260C>G (p.Pro87Arg)	SCN3B (P87R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1436068	NM_001040151.2(SCN3B):c.233G>A (p.Arg78Gln)	SCN3B (R78Q)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +1 more	GUncertain significance
Select item 432438	NM_001040151.2(SCN3B):c.199G>A (p.Glu67Lys)	SCN3B (E67K)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 140596	NM_001040151.2(SCN3B):c.161T>G (p.Val54Gly)	SCN3B (V54G)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 1376285	NM_001040151.2(SCN3B):c.106G>A (p.Val36Met)	SCN3B (V36M)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +1 more	GConflicting classifications of pathogenicity
Select item 582724	NM_001040151.2(SCN3B):c.98C>T (p.Thr33Met)	SCN3B (T33M)	Single nucleotide variant (missense variant)	Brugada syndrome 7 +1 more	GUncertain significance
Select item 303208	NM_001040151.2(SCN3B):c.-62del	SCN3B	Deletion (5 prime UTR variant)	Brugada syndrome +1 more	GUncertain significance